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FDA 510(k)

SIRESKOP SX

K-Number: K951358 · 1995-05-15

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1995-05-15
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIRESKOP SX is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1995-05-15 under 510(k) number K951358. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIRESKOP SX?

SIRESKOP SX is a medical device that received FDA 510(k) clearance on 1995-05-15. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K951358.

When did SIRESKOP SX receive FDA 510(k) clearance?

SIRESKOP SX received FDA 510(k) clearance on 1995-05-15, under 510(k) number K951358.

Who is the listed applicant for SIRESKOP SX?

The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIRESKOP SX?

The FDA product code for SIRESKOP SX is JAA.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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